Low Growth Hormone Levels in Short-Stature Children with Pituitary Hyperplasia Secondary to Primary Hypothyroidism

Objective. The follow-up of GH levels in short-stature children with pituitary hyperplasia secondary to primary hypothyroidism (PPH) is reported in a few cases. We aimed to observe changes in GH secretion in short-stature children with PPH. Methods. A total of 11 short-stature children with PPH acco...

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Main Authors: Minghua Liu, Yanyan Hu, Guimei Li, Wenwen Hu
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:International Journal of Endocrinology
Online Access:http://dx.doi.org/10.1155/2015/283492
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author Minghua Liu
Yanyan Hu
Guimei Li
Wenwen Hu
author_facet Minghua Liu
Yanyan Hu
Guimei Li
Wenwen Hu
author_sort Minghua Liu
collection DOAJ
description Objective. The follow-up of GH levels in short-stature children with pituitary hyperplasia secondary to primary hypothyroidism (PPH) is reported in a few cases. We aimed to observe changes in GH secretion in short-stature children with PPH. Methods. A total of 11 short-stature children with PPH accompanied by low GH levels were included. They received levothyroxine therapy after diagnosis. Their thyroid hormones, IGF-1, PRL, and pituitary height were measured at baseline and 3 months after therapy. GH stimulation tests were performed at baseline and after regression of thyroid hormones and pituitary. Results. At baseline, they had decreased GH peak and FT3 and FT4 levels and elevated TSH levels. Decreased IGF-1 levels were found in seven children. Elevated PRL levels and positive thyroid antibodies were found in 10 children. The mean pituitary height was 14.3±3.8 mm. After 3 months, FT3, FT4, and IGF-1 levels were significantly increased (all p<0.01), and values of TSH, PRL, and pituitary height were significantly decreased (all p<0.001). After 6 months, pituitary hyperplasia completely regressed. GH levels returned to normal in nine children and were still low in two children. Conclusion. GH secretion can be resolved in most short-stature children with PPH.
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spelling doaj-art-cdf4f0e77fdb41baa7beb53666e1c7f82025-08-20T02:19:27ZengWileyInternational Journal of Endocrinology1687-83371687-83452015-01-01201510.1155/2015/283492283492Low Growth Hormone Levels in Short-Stature Children with Pituitary Hyperplasia Secondary to Primary HypothyroidismMinghua Liu0Yanyan Hu1Guimei Li2Wenwen Hu3Department of Pediatrics, Shandong Provincial Hospital Affiliated to Shandong University, 9677 Jingshi Road, Jinan, Shandong 250014, ChinaDepartment of Pediatrics, Shandong Provincial Hospital Affiliated to Shandong University, 9677 Jingshi Road, Jinan, Shandong 250014, ChinaDepartment of Pediatrics, Shandong Provincial Hospital Affiliated to Shandong University, 9677 Jingshi Road, Jinan, Shandong 250014, ChinaDepartment of Pediatrics, The People’s Hospital of Lanshan District, 51 Lanshan Road, Linyi, Shandong 276000, ChinaObjective. The follow-up of GH levels in short-stature children with pituitary hyperplasia secondary to primary hypothyroidism (PPH) is reported in a few cases. We aimed to observe changes in GH secretion in short-stature children with PPH. Methods. A total of 11 short-stature children with PPH accompanied by low GH levels were included. They received levothyroxine therapy after diagnosis. Their thyroid hormones, IGF-1, PRL, and pituitary height were measured at baseline and 3 months after therapy. GH stimulation tests were performed at baseline and after regression of thyroid hormones and pituitary. Results. At baseline, they had decreased GH peak and FT3 and FT4 levels and elevated TSH levels. Decreased IGF-1 levels were found in seven children. Elevated PRL levels and positive thyroid antibodies were found in 10 children. The mean pituitary height was 14.3±3.8 mm. After 3 months, FT3, FT4, and IGF-1 levels were significantly increased (all p<0.01), and values of TSH, PRL, and pituitary height were significantly decreased (all p<0.001). After 6 months, pituitary hyperplasia completely regressed. GH levels returned to normal in nine children and were still low in two children. Conclusion. GH secretion can be resolved in most short-stature children with PPH.http://dx.doi.org/10.1155/2015/283492
spellingShingle Minghua Liu
Yanyan Hu
Guimei Li
Wenwen Hu
Low Growth Hormone Levels in Short-Stature Children with Pituitary Hyperplasia Secondary to Primary Hypothyroidism
International Journal of Endocrinology
title Low Growth Hormone Levels in Short-Stature Children with Pituitary Hyperplasia Secondary to Primary Hypothyroidism
title_full Low Growth Hormone Levels in Short-Stature Children with Pituitary Hyperplasia Secondary to Primary Hypothyroidism
title_fullStr Low Growth Hormone Levels in Short-Stature Children with Pituitary Hyperplasia Secondary to Primary Hypothyroidism
title_full_unstemmed Low Growth Hormone Levels in Short-Stature Children with Pituitary Hyperplasia Secondary to Primary Hypothyroidism
title_short Low Growth Hormone Levels in Short-Stature Children with Pituitary Hyperplasia Secondary to Primary Hypothyroidism
title_sort low growth hormone levels in short stature children with pituitary hyperplasia secondary to primary hypothyroidism
url http://dx.doi.org/10.1155/2015/283492
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AT guimeili lowgrowthhormonelevelsinshortstaturechildrenwithpituitaryhyperplasiasecondarytoprimaryhypothyroidism
AT wenwenhu lowgrowthhormonelevelsinshortstaturechildrenwithpituitaryhyperplasiasecondarytoprimaryhypothyroidism